rs2076059
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2076059(C;C) |
Make rs2076059(C;T) |
Make rs2076059(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 1 |
Position | 169729780 |
Gene | SELE |
is a | snp |
is | mentioned by |
dbSNP | rs2076059 |
dbSNP (classic) | rs2076059 |
ClinGen | rs2076059 |
ebi | rs2076059 |
HLI | rs2076059 |
Exac | rs2076059 |
Gnomad | rs2076059 |
Varsome | rs2076059 |
LitVar | rs2076059 |
Map | rs2076059 |
PheGenI | rs2076059 |
Biobank | rs2076059 |
1000 genomes | rs2076059 |
hgdp | rs2076059 |
ensembl | rs2076059 |
geneview | rs2076059 |
scholar | rs2076059 |
rs2076059 | |
pharmgkb | rs2076059 |
gwascentral | rs2076059 |
openSNP | rs2076059 |
23andMe | rs2076059 |
SNPshot | rs2076059 |
SNPdbe | rs2076059 |
MSV3d | rs2076059 |
GWAS Ctlg | rs2076059 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 25711033] [Association between inflanummatory gene polymorphisms and the risk of myocardial infarction]
[PMID 25945941] Polymorphisms of inflammatory markers and risk of essential hypertension in Tatars from Russia
[PMID 26662939] Genotype/allelic combinations as potential predictors of myocardial infarction.